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EP2655702B1 - Substrat avec un revêtement résistant à la corrosion et son procédé de fabrication - Google Patents

Substrat avec un revêtement résistant à la corrosion et son procédé de fabrication Download PDF

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Publication number
EP2655702B1
EP2655702B1 EP11804965.9A EP11804965A EP2655702B1 EP 2655702 B1 EP2655702 B1 EP 2655702B1 EP 11804965 A EP11804965 A EP 11804965A EP 2655702 B1 EP2655702 B1 EP 2655702B1
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EP
European Patent Office
Prior art keywords
layer
nickel
tin
chromium
salt
Prior art date
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Revoked
Application number
EP11804965.9A
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German (de)
English (en)
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EP2655702A1 (fr
Inventor
Gianluigi SCHIAVON
Diego DAL ZILIO
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Coventya SpA
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Coventya SpA
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Priority to PL11804965T priority Critical patent/PL2655702T3/pl
Publication of EP2655702A1 publication Critical patent/EP2655702A1/fr
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Revoked legal-status Critical Current
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/60—Electroplating characterised by the structure or texture of the layers
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/10—Electroplating with more than one layer of the same or of different metals
    • C25D5/12—Electroplating with more than one layer of the same or of different metals at least one layer being of nickel or chromium
    • C25D5/14—Electroplating with more than one layer of the same or of different metals at least one layer being of nickel or chromium two or more layers being of nickel or chromium, e.g. duplex or triplex layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00—Layered products comprising a layer of metal
    • B32B15/01—Layered products comprising a layer of metal all layers being exclusively metallic
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/60—Electroplating characterised by the structure or texture of the layers
    • C25D5/623—Porosity of the layers
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/60—Electroplating characterised by the structure or texture of the layers
    • C25D5/625—Discontinuous layers, e.g. microcracked layers
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/627—Electroplating characterised by the visual appearance of the layers, e.g. colour, brightness or mat appearance
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/12—All metal or with adjacent metals
    • Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
    • Y10T428/12771—Transition metal-base component
    • Y10T428/12806—Refractory [Group IVB, VB, or VIB] metal-base component
    • Y10T428/12826—Group VIB metal-base component
    • Y10T428/12847—Cr-base component
    • Y10T428/12854—Next to Co-, Fe-, or Ni-base component

Definitions

  • the invention relates to a substrate with a corrosion resistant coating which comprises at least one nickel layer and, as finish, at least one chromium layer. Between these layers, a tin-nickel alloy layer is deposited for suppression of corrosion reactions.
  • the invention also relates to a method of production of such substrates with corrosion resistant coating.
  • Electrolytic chromium and nickel depositions are generally chosen for realizing of a high corrosion resistance.
  • the nickel layer is divided in three different types.
  • the first type is known as semi-bright nickel layer or sulfur-free layer, because it is a semi-bright layer having a sulfur content ⁇ 0.005 weight-%. These layers have a higher electrochemical potential than bright nickel layers.
  • a bright nickel layer is regularly electroplated. This leads to a bright appearance of the coated articles.
  • These layers have a sulfur content of more than 0.03 weight-%.
  • the last nickel layer is a layer which has small disruptions on a micro-scale.
  • This layer can comprise micro-particles or organic additives and can be coated with a chromium layer which has a micro-porous layer or a layer with micro cracks.
  • These layers are usually nobler than bright nickel layers i.e. their potential is higher than that of bright nickel layers.
  • Such coatings are known from US 3,268,424 and US 3,563,864 .
  • the main aim is to decrease galvanic corrosion between chromium and nickel.
  • the chromium layer is thereby electroplated as finish with an electrolyte comprising hexavalent chromium.
  • EP 1 343 924 B1 discloses a layer of silver or silver alloy which is located between the chromium and nickel layer. It is a problem that very toxic cyanide salts are used in the process which represent a serious threat for health and safety and are therefore no longer acceptable with regard to environmental aspects. Furthermore, silver as noble metal demonstrates two important disadvantages which are the high cost as well as the significant difference of the electrochemical potential in comparison to a bright nickel layer.
  • Trivalent chromium electrolytes have been used for years as decorative coatings, but show the disadvantage that they do not demonstrate sufficient corrosion resistance because it is not a pure chromium layer, but a special alloy comprising constituents of chromium, carbon, iron, sulfur, oxygen and nitrogen and thus have structural features different to pure chromium.
  • the UNI EN ISO 9227 CASS standard procedure (so-called CASS test) is applied for the investigation of the corrosion resistance of coated parts. In this test, the corrosion resistance (in hours) is measured in a room filled with salt spray at 50 °C, wherein the salt consists of a sodium chloride solution which comprises copper ions with acetic acid (pH 3).
  • a substrate with a corrosion resistant coating which comprises at least one nickel layer and at least one chromium layer as finish. Between a nickel layer and a proximate chromium layer, at least one tin-nickel alloy layer is deposited for the suppression of corrosion reactions.
  • a suppression of corrosion reactions also means an essential or significant reduction of corrosion reactions.
  • the inventive idea for increasing corrosion resistance is based on replacing the prior art nickel layer having micro-scale disruptions with a tinnickel alloy layer.
  • This tin-nickel alloy layer enables the use of a variety of chromium-containing electrolytes for galvanic deposition of a chromium finish.
  • Tin-nickel alloys with an increased amount of tin have good corrosion resistance and are often used as coating for prevention of surface clouding.
  • the corrosion rate between nickel and chromium layers during the corrosion test UNI EN ISO 9227 NSS or UNI EN ISO 9227 CASS can be reduced.
  • the present invention allows that corrosion, which arises due to the use of antifreeze and particularly affects automotive components which are exposed to the weather during winter, can be drastically reduced.
  • significantly improved results could be achieved in the mentioned standard tests of VW (VW PV1067) and Nissan (NES M4063) compared to methods for corrosion protection known in the prior art.
  • the tin-nickel alloy layer comprises preferably 55 to 75 weight-%, more preferably 60 to 70 weight-% and most preferably 64 to 68 weight-% tin and preferably 45 to 25 weight-%, more preferably 40 to 30 weight-% and most preferably 36 to 32 weight-% nickel.
  • a layer of this alloy has a grey-pink color, as it is known from the ISO 2179:1986 standard.
  • the tin-nickel alloy layer preferably has a thickness in the range of 0.1 ⁇ m to 10 ⁇ m, more preferably 0.2 ⁇ m to 6 ⁇ m and most preferably 0.5 ⁇ m to 5 ⁇ m.
  • the at least one nickel layer preferably has a thickness of 1 to 50 ⁇ m.
  • the at least one chromium layer preferably has a thickness of 0.05 to 2 ⁇ m.
  • the coating consists of a bright nickel layer which is deposited on the substrate or a further metallic layer as well as the tin-nickel alloy layer and the chromium layer.
  • the further metallic layer herewith preferably consists of copper or essentially comprises copper.
  • a further semi-bright nickel layer is arranged between the bright nickel layer and the substrate or the further metallic layer.
  • the inventive coating can be combined with almost any number of substrate materials.
  • substrates of a metal or a metal alloy, particularly steel, brass or an aluminium alloy.
  • zinc die cast elements can be provided with the inventive coating.
  • Further materials are selected from the group consisting of plastics, in particular acrylnitril-butadien-styrol (ABS), acrylnitril-butadien-styrol/polycarbonate (ABS-PC), polypropylene (PP) or polyamide (PA).
  • ABS acrylnitril-butadien-styrol
  • ABS-PC acrylnitril-butadien-styrol/polycarbonate
  • PP polypropylene
  • PA polyamide
  • a corrosion resistant coating for a substrate wherein the following layers are electroplated on the substrate subsequently:
  • c) is one chromium layer which is a electroplated finish, i.e. the last electroplated layer of the corrosion resistant coating. This does not exclude that at least one further non-metallic layer is deposited on the chromium finish, e.g. an organic or inorganic passivation or a sealing.
  • a first preferred variant provides that the at least one tin-nickel alloy layer is electroplated from an acidic aqueous electrolyte with a pH in the range of 2 to 6.
  • the electrolyte comprises at least one tin salt and at least one nickel salt.
  • the electrolyte can comprise fluorides or chlorides which act as activators of the nickel layer for an improved adhesion of the tin-nickel alloy layer on the nickel layer.
  • fluoroborates, methanesulfonate and sulfates can be comprised.
  • the at least one tin-nickel alloy layer is electroplated from an alkaline aqueous electrolyte, wherein the electrolyte comprises at least one tin salt and at least one nickel salt and the salts are particularly selected from the group consisting of sulfates, sulfamates, phosphates, pyrophosphate, glycine, and mixtures thereof.
  • the at least one tin-nickel alloy layer is electroplated from a neutral aqueous electrolyte, wherein the electrolyte comprises at least one tin salt and at least one nickel salt and the salts are particularly selected from the group consisting of sulfates, sulfamates, phosphates, pyrophosphate, glycine, and mixtures thereof.
  • the at least one tin-nickel alloy layer is electroplated from a cyanide-containing aqueous electrolyte, wherein the electrolyte comprises at least one tin salt and at least one nickel salt are particularly selected from the group consisting of sulfates, sulfamates, phosphates, pyrophosphate, glycine, and mixtures thereof.
  • the cyanide containing electrolyte can comprise the following further additives:
  • aqueous electrolytes for tin-nickel can comprise the following further additives:
  • the tin salts used according to the invention are preferably selected from the group consisting of chlorides, fluorides, fluoroborates, sulfates, methane sulfonates and mixtures thereof and the nickel salt is preferably selected from the group consisting of chlorides, fluorides, fluoroborates, sulfates, sulfamates, pyrophosphates, methane sulfonates, and mixtures thereof.
  • an electroplating from an acidic aqueous electrolyte is carried out, wherein the electrolyte comprises chromium(VI)-salts, in particular chromic acid.
  • the electroplating is carried out from an acidic aqueous electrolyte, wherein the electrolyte comprises chromium(III)-salts, in particular chromium(III)-sulfate or chromium(III)-chloride, which are preferred because of environmental aspects.
  • the chromium deposit can comprise 1 to 25 weight-% carbon, 1 to 30 weight-% oxygen, 0 to 10 weight-% sulfur, 0 to 10 weight-% nitrogen and 0 to 30 weight-% iron.
  • ABS acrylonitrile-butadienestyrene
  • the coatings according to the invention were deposited from an electrolyte with the following composition and parameters: NiCl 2 *6H 2 O 200-300 g/l NH 4 HF 2 30-80 g/l SnCl 2 *2H 2 O 20-60 g/l pH 2-5 temperature 40-60°C
  • the coating was deposited from an electrolyte with the following composition and parameters: NiCl 2 *6H 2 O 200-300 g/l NH 4 HF 2 30-80 g/l SnCl 2 *2H 2 0 20-60 g/l Diethylenetriamine 20-100g/l pH 3.8-5.5 Temperature 40-60°C
  • Electrolytes were used for the deposition of a chromium(III)-layer. These electrolytes are distributed under the names TRISTAR 300, TRISTAR 300 AF, TRISTAR 700 and TRISTAR 720 by the company Coventya.
  • the TRISTAR 300 process is a chloride-based process and provides a white chromium layer wherein the electrolyte has the following composition and parameters: Cr 3+ 15-25 g/l organic acid 25-250 g/l Conducting salts 150-300 g/l pH 2-6 temperature 25-35°C
  • the TRISTAR 700 process is comparable with the process described before wherein a chromium layer with a darker coloration results.
  • the electrolyte used herein has the following composition and parameters: Cr 3+ 15-25 g/l organic acid 25-50 g/l conducting salts 150-300 g/l blackening agent 1-10 g/l pH 2-3 temperature 25-35°C
  • the TRISTAR 300 AF process is a sulfate-based process and results in a chromium layer with white color.
  • the electrolyte comprises the following composition and parameters: Cr 3+ 5-15 g/l organic acid 5-20 g/l conducting salts 150-300 g/l pH 3-4 temperature 45-65°C
  • the TRISTAR 720 process is comparable to the TRISTAR 300 AF process, but results in a chromium layer with darker coloration.
  • the electrolyte comprises the following composition and parameters: Cr 3+ 5-15 g/l organic acid 5-20 g/l conducting salts 150-300 g/l blackening agent 2-10 g/l pH 3-4 temperature 45-65°C
  • a first corrosion test according to UNI EN ISO 9227 CASS was carried out with such produced samples.
  • the duration of the test was 24, 48, 72, 96 and 120 hours.
  • the samples were evaluated during the second corrosion test with calcium chloride at the end of the test (after 48 hours). The samples were cleaned and dried without damaging the surface. Any change of the surface could be also monitored exactly.
  • samples A, C, E, G and I are those which represent the prior art. These samples comprise a nickel layer with micro-scale disruptions as intermediate layer between the bright nickel layer and the chromium finish.
  • Examples B, D and D', F, F', H, L and L' are coatings according to the invention and comprise a tin-nickel alloy layer between the bright nickel layer and the chromium finish.
  • sample B demonstrates a better corrosion resistance compared to sample A both in CASS test and CaCl2 test.
  • Sample D and D' demonstrates a better corrosion resistance compared to sample C both in CASS test and CaCl2 test.
  • Sample F and F' demonstrates a better corrosion resistance compared to sample E both in CASS test and CaCl2 test.
  • Sample H demonstrates a better corrosion resistance compared to sample G both in CASS test and CaCl2 test.
  • Sample L and L' demonstrates a better corrosion resistance compared to sample I both in CASS test and CaCl2 test.
  • samples D, D', F and F' demonstrate excellent results and pass both the 96-hours CASS-test and the 48-hours VW PV1067 standard test. More particularly the sample D', F' showed the best corrosion resistance to CASS test passing both the 120h.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electroplating Methods And Accessories (AREA)
  • Chemically Coating (AREA)
  • Physical Vapour Deposition (AREA)
  • Electroplating And Plating Baths Therefor (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)

Claims (13)

  1. Substrat avec un revêtement résistant à la corrosion,
    dans lequel le revêtement comprend au moins une couche de nickel brillant et au moins une couche de chrome en tant que couche de finition,
    caractérisé en ce qu'entre la couche de nickel brillant, qui est déposée sur le substrat ou une autre couche métallique, et la couche de chrome, au moins une couche d'un alliage d'étain-nickel est déposée pour supprimer les réactions de corrosion et les couches sont électroplaquées.
  2. Substrat selon la revendication 1,
    caractérisé en ce que l'alliage d'étain-nickel se compose de 55 à 75 % en poids, de préférence de 60 à 70 % en poids, plus préférablement de 64 à 68 % en poids d'étain et de 45 à 25 % en poids, de préférence de 40 à 30 % en poids, plus préférablement de 36 à 32 % en poids de nickel.
  3. Substrat selon l'une quelconque des revendications précédentes, caractérisé en ce que la couche de l'au moins un alliage d'étain-nickel a une épaisseur de 0,1 à 10 µm, de préférence de 0,2 à 6 µm, plus préférablement de 0,5 à 5 µm et/ou la couche de nickel a une épaisseur de 1 à 50 µm et/ou la couche de chrome a une épaisseur de 0,05 à 2 µm.
  4. Substrat selon l'une quelconque des revendications précédentes, caractérisé en ce que l'autre couche métallique se compose de cuivre ou comprend essentiellement du cuivre.
  5. Substrat selon l'une quelconque des revendications précédentes, caractérisé en ce qu'une couche de nickel semi-brillant est arrangée entre la couche de nickel brillant et le substrat ou l'autre couche métallique.
  6. Substrat selon l'une quelconque des revendications précédentes, caractérisé en ce que le substrat se compose d'un métal ou d'un alliage métallique, en particulier d'acier, de laiton, d'un alliage d'aluminium ou d'un zinc moulé sous pression, ou de plastiques, en particulier d'acrylonitrile-butadiène-styrol (ABS), d'acrylonitrile-butadiène-styrol/polycarbonate (ABS-PC), de polypropylène (PP) ou de polyamide (PA).
  7. Procédé de production d'un revêtement résistant à la corrosion pour un substrat, dans lequel les couches suivantes sont électroplaquées subséquemment :
    a) au moins une couche de nickel brillant,
    b) au moins une couche d'alliage d'étain-nickel, et
    c) au moins une couche de chrome en tant que couche de finition,
    dans lequel les réactions de corrosion sont supprimées par la couche d'alliage d'étain-nickel.
  8. Procédé selon la revendication 7, caractérisé en ce que l'au moins une couche d'alliage d'étain-nickel est électroplaquée à partir d'un électrolyte aqueux acide ayant un pH compris dans la plage allant de 2 à 6, l'électrolyte comprenant des additifs, en particulier des chlorures, des fluorures, des fluoroborates mis à part ceux d'au moins un sel d'étain et d'au moins un sel de nickel ou à partir d'un électrolyte aqueux alcalin, l'électrolyte comprenant au moins un sel d'étain et au moins un sel de nickel, les sels étant en particulier choisis dans le groupe constitué par les sulfates, les sulfamates, les phosphates, les pyrophosphates, la glycine, et des mélanges de ceux-ci ou à partir d'un électrolyte aqueux contenant du cyanure, l'électrolyte comprenant au moins un sel d'étain et au moins un sel de nickel, les autres sels étant en particulier choisis dans le groupe constitué par les sulfates, les sulfamates, les phosphates, les pyrophosphates, la glycine, et des mélanges de ceux-ci ou à partir d'un électrolyte aqueux faiblement alcalin ayant un pH compris dans la plage allant de 6 à 10, l'électrolyte comprenant au moins un sel d'étain et au moins un sel de nickel, les sels étant en particulier choisis dans le groupe constitué par les sulfates, les sulfamates, les phosphates, les pyrophosphates, la glycine, et des mélanges de ceux-ci.
  9. Procédé selon la revendication 7 ou 8,
    caractérisé en ce que l'électrolyte comprend en outre des additifs choisis dans le groupe constitué par
    - les agents complexants, de préférence les amines, les polyamines, de préférence choisis dans le groupe constitué par l'éthylènediamine, la diéthylènetriamine, la triéthylènetétramine, la tétraéthylènepentamine, l'aminoéthyléthanolamine, la triéthanolamine, la diéthanolamine, la monoéthanolamine, ainsi que leurs combinaisons avec des acides organiques, de préférence choisis dans le groupe constitué par l'acide citrique, l'acide tartrique et l'acide lactique ;
    - des agents mouillants, en particulier des tensioactifs amphotères, anioniques, cationiques ou non ioniques ;
    - des mélanges de ceux-ci.
  10. Procédé selon l'une quelconque des revendications 7 à 9, caractérisé en ce que le sel d'étain est choisi dans le groupe constitué par les chlorures, les fluorures, les fluoroborates, les sulfates, les méthanesulfonates et des mélanges de ceux-ci, et le sel de nickel est choisi dans le groupe constitué par les chlorures, les fluorures, les fluoroborates, les sulfates, les sulfamates, les pyrophosphates, les méthanesulfonates et des mélanges de ceux-ci.
  11. Procédé selon l'une quelconque des revendications 7 à 10, caractérisé en ce qu'au moins une couche de chrome est électroplaquée à partir d'un électrolyte aqueux acide, l'électrolyte comprenant au moins un sel de chrome(VI), en particulier de l'acide chromique (CrO3).
  12. Procédé selon l'une quelconque des revendications 7 à 11, caractérisé en ce qu'au moins une couche de chrome est électroplaquée à partir d'un électrolyte aqueux acide ayant un pH compris dans la plage allant de 2 à 6, l'électrolyte comprenant au moins un sel de chrome(III), en particulier le sulfate de chrome ou le chlorure de chrome.
  13. Procédé selon la revendication 12, caractérisé en ce que l'électrolyte comprend en outre des additifs choisis dans le groupe constitué par :
    - des acides organiques, en particulier l'acide formique, l'acide acétique, l'acide aminoacétique, l'acide oxalique, l'acide malique, l'acide aspartique et des sels de ceux-ci ;
    - des acides inorganiques, en particulier l'acide borique, l'acide chlorhydrique, l'acide sulfurique et des sels de ceux-ci ;
    - des sels conducteurs, en particulier le chlorure de sodium, le chlorure de potassium, le chlorure d'ammonium, le sulfate de sodium, le sulfate de potassium, le sulfate d'ammonium, le bromure de sodium, le bromure de potassium, le bromure d'ammonium, le sulfate de fer, le chlorure de fer ou l'hypophosphite de sodium ;
    - des additifs, y compris des agents noircissants, en particulier une thiourée et d'autres composés organosulfurés, l'urée, le thiocyanate de sodium, le thiocyanate de potassium, le thiocyanate d'ammonium, un sel sodique de saccharine, le vinylsulfonate de sodium, les polymères cationiques ;
    - des agents mouillants, en particulier des tensioactifs amphotères, anioniques, cationiques ou non ioniques.
EP11804965.9A 2010-12-23 2011-12-23 Substrat avec un revêtement résistant à la corrosion et son procédé de fabrication Revoked EP2655702B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL11804965T PL2655702T3 (pl) 2010-12-23 2011-12-23 Podłoże z powłoką odporną na korozję i sposób jego wytwarzania

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DE102010055968A DE102010055968A1 (de) 2010-12-23 2010-12-23 Substrat mit korrosionsbeständigem Überzug und Verfahren zu dessen Herstellung
PCT/EP2011/006547 WO2012084262A1 (fr) 2010-12-23 2011-12-23 Substrat doté d'un revêtement résistant à la corrosion et son procédé de production

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EP2655702A1 EP2655702A1 (fr) 2013-10-30
EP2655702B1 true EP2655702B1 (fr) 2016-04-06

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EP11804965.9A Revoked EP2655702B1 (fr) 2010-12-23 2011-12-23 Substrat avec un revêtement résistant à la corrosion et son procédé de fabrication

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US (1) US10011913B2 (fr)
EP (1) EP2655702B1 (fr)
JP (1) JP2014500404A (fr)
KR (1) KR20140044768A (fr)
CN (1) CN103339296B (fr)
BR (1) BR112013015815A2 (fr)
CA (1) CA2822476C (fr)
DE (1) DE102010055968A1 (fr)
DK (1) DK2655702T3 (fr)
ES (1) ES2569991T3 (fr)
MX (1) MX362153B (fr)
PL (1) PL2655702T3 (fr)
WO (1) WO2012084262A1 (fr)

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DE102010055968A1 (de) 2010-12-23 2012-06-28 Coventya Spa Substrat mit korrosionsbeständigem Überzug und Verfahren zu dessen Herstellung
CN102912387A (zh) * 2012-10-26 2013-02-06 南京大地冷冻食品有限公司 一种氯化物型三价铬镀黑铬镀液
CN102888601A (zh) * 2012-10-26 2013-01-23 南京大地冷冻食品有限公司 一种镀锌层三价铬黑钝镀液
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JP2014500404A (ja) 2014-01-09
EP2655702A1 (fr) 2013-10-30
PL2655702T3 (pl) 2016-08-31
WO2012084262A1 (fr) 2012-06-28
CN103339296A (zh) 2013-10-02
US20140127532A1 (en) 2014-05-08
DK2655702T3 (en) 2016-05-17
CN103339296B (zh) 2017-02-08
ES2569991T3 (es) 2016-05-13
BR112013015815A2 (pt) 2018-05-15
US10011913B2 (en) 2018-07-03
KR20140044768A (ko) 2014-04-15
CA2822476C (fr) 2016-12-13

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